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Chemoenzymatic route to stereodefined 2-(azidophenyl)oxazolines for click chemistry
Aryl-substituted esters of a racemic diprotected 2-azido-1-alkanol were submitted to the Staudinger/aza-Wittig reaction in order to assess scope and establish conditions for their cyclization to the corresponding 2,4,5-trisubstituted oxazolines. Following the cyclization study, the (2R,3R)-antipode...
Guardat en:
| Publicat a: | Tetrahedron Lett |
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| Autors principals: | , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
2020
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7946107/ https://ncbi.nlm.nih.gov/pubmed/33716327 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.tetlet.2020.152717 |
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